Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Cross Contamination


Aimee D.

Recommended Posts

Aimee D. Newbie

I have recently been diagnosed with celiacs (2 1/2 months ago) and I have not seen any drastic improvements on the way I feel. I think I am cross contaminating myself with the things that I feed my 2 yr old. We are always so close and he loves to touch everything on my face and give me kisses. I love this of coarse and want him to be close. I am not sure how to stop this from happening and I am so frustrated and tired. I have been looking so forward to being more energetic and having less headaches, but its just not happining, and I am really trying hard. I've reduced my diet to gluten-free tuna and gluten-free mayo (only I use), gluten-free peanut butter, fish fillets (clean pan, cooked in olive oil), crab legs, salad w/ gluten-free dressing, diet red bull, orange juice and water. I also take supplements that are labled hypo allergenic w/ no wheat or gluten. I'm pretty sure these foods do not contain gluten and I don't mind only eating them because I'm not that hungry anyway. I also only use gluten free shampoo, cleansing products moisturizers and make-up. I have checked all of it, or ordered it special off the internet.

I am not sure it is wise to not feed my son gluten, but I might have to go that route. If there is any insight or suggestions I could really use some help.

Thanks


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



happygirl Collaborator

Hey Aimee,

Welcome to the board! We are happy you have found us! It is a great resource and I hope it provides you with education and support.

Let's see--first, how were you diagnosed with Celiac Disease (Celiac, without the "s")? Through bloodwork, biopsy, or both? I noticed in your signature that you have diabetes, which is highly correlated with Celiac https://www.celiac.com/st_prod.html?p_prodid=1405. What types of symptoms do you have that lead you/your doctor to determine you have Celiac---and what symptoms do you currently have that are not going away? How sick were/are you? (Just trying to get a little information so we can help)

But, without knowing your circumstances, there are a couple standard things. Since you have *only* been gluten free for 2.5 months (although it might seem like a lifetime---I understand!), your body is very potentially still healing. It is a process to start to feel better---for many, it can still take a few months or longer, even though they are strictly gluten free. It sounds like you are very thorough with your ingredients and most areas of cross contamination. However, I will say that I would not be comfortable with the things your sweet son does. I have a niece your son's age, and she must finish her meal, wash her hands, and then we resume playtime. I can't say that it is your *only* problem, but it is a risk for contamination-you are correct. Doesn't mean that it will get into your system every time, but .... its something you'll have to decide. Have you spoken to your doctor about this? Do you have a doctor that is knowledgable about Celiac and educated about it?

By the way, putting your son on a gluten free diet is not harmful, if you choose to do that. Speaking of that, it is recommended by Celiac experts that all first degree relatives are tested for Celiac. Although he is rather young and testing is not as reliable for children under 2, it would be advisable in the future (and, if it is negative, it still needs to be run periodically throughout his life, even with no symptoms).

Good luck and I hope you start to improve. Let us know what we can do to help!

Laua

Aimee D. Newbie
I have recently been diagnosed with celiacs (2 1/2 months ago) and I have not seen any drastic improvements on the way I feel. I think I am cross contaminating myself with the things that I feed my 2 yr old. We are always so close and he loves to touch everything on my face and give me kisses. I love this of coarse and want him to be close. I am not sure how to stop this from happening and I am so frustrated and tired. I have been looking so forward to being more energetic and having less headaches, but its just not happining, and I am really trying hard. I've reduced my diet to gluten-free tuna and gluten-free mayo (only I use), gluten-free peanut butter, fish fillets (clean pan, cooked in olive oil), crab legs, salad w/ gluten-free dressing, diet red bull, orange juice and water. I also take supplements that are labled hypo allergenic w/ no wheat or gluten. I'm pretty sure these foods do not contain gluten and I don't mind only eating them because I'm not that hungry anyway. I also only use gluten free shampoo, cleansing products moisturizers and make-up. I have checked all of it, or ordered it special off the internet.

I am not sure it is wise to not feed my son gluten, but I might have to go that route. If there is any insight or suggestions I could really use some help.

Thanks

Thank you, OOPS... sorry for the misspell!

I had both, positive blood work and a biopsy that showed spru in my stomach.

After I gave birth to my 2nd son I breast fed him for about 6 mo. and after that I kept expecting to get over the side effects of the pregnancy and the breast feeding, but I just kept feeling nauseous and tired. My husband and I had just moved to Alaska via the Air Force, so I got aquainted with my general physician who quickley refered me to an endocrinologists off base. I complained about the stomache discomfort to him and he asked if I had ever been tested for celiac disease. I told him not that I was aware of, I really didn't even know what he was talking about. He is fresh from India and has a strong accent. Three months later when I revisited him he told me the test he ran showed just slightly elevated antibody levels, but he thought I should get a referal to a GI just to make sure I didn't have celiac disease. I still was not sure what he was talking about. In the meantime I had gone for a dental checkup because I knew I needed to have a cavity filled that a dentist had found prior to our move. I was quickley side tracked by extensive and excessive ongoing dental work. At that time I had 12 unfilled cavities and needed 1 root canal. (Just one year later I have had a total of eight root canals and still need work.) I still had not researched anything on celiac disease, and revisited the endocrinologist for more routine bloodwork at which time he still persisted I check into having my stomache looked at. So I went to the general physician and requested a GI DR. and at that time I Had a constant headache that had not gone away for about three months straight. (I thought this was because of the dental work, turns out it was celiac disease) I went to a chiropractor because I was having hip, back and neck pain prior to the biopsy and wrote on the info sheet that I had celiac disease. The chiropractor happened to be well versed on celiac disease and diabetes. He had written a paper on celiac disease while he was in college. He explained to me what I would need to do and where to get info from the internet. I tried it for about 2 days and then decided I would make that appointment and ask for the biopsy! It took about 3 more months to get the test and the results and when the GI called me with the results all I could do was cry.

From that point on I have been on my own with this and it has been a lot of trial and error, and a lot of mistakes. I have gotten tons of ideas and info from this site. I know for a fact that I glutened myself last Tuesday when I ate a mixed bag of nuts and raisins w/ out reading the ingredients. So then I was so frustrated and I knew I had already blown it, so I went out for chinese w/ my husband and enjoyed everything gluten I could find, including beer. I didn't feel bad the next day or so, but now I'm very irritable and edgy, I want to bite everybodies head off and I cry lots and I have a bad headache. This could be from lack of sunshine, but I'm usually a fairly stable person in general.

ravenwoodglass Mentor

Hello and welcome. I just wanted to address the issue of making your home gluten free. It is not going to be harmful at all to make gluten off limits in your home.

Your DS is not more likely to become celiac if you do this, it will however make it obvious if he needs to be on the diet when he is out and comsuming gluten. This is not a bad thing. There is a good chance that he has also got the genes for celiac but keeping him gluten free at home is not going to cause it.

I wish I had known early on, it took over 15 years for me to be diagnosed and the damage that was done to my children because they never looked for it was substantial. That damage included growth stunting and emotional and learning problems. If I could go back in time and know what I do now I would never allow this toxin into my or my childrens lives. Even if they had only been gluten-free at home before they went to school things would have been very different.

My son had gluten shoved down his throat from the time he was 6 months old, but the fact he was only 12 lbs at a year didn't concern the doctors. I would not hesitate to reccommend strongly that you make your home gluten free. You may not know your son needs to be also until it is too late.

Jestgar Rising Star

Hi Aimee,

I agree with making your house gluten free. You can use this as an opportunity to teach your kids about the value of reading labels and understanding what goes into their bodies. You can explain to your kids about chemicals and additives and how some foods make mommy sick so she tries to not eat foods that aren't healthy, and she never eats the foods that make her sick.

If they grow up understanding how food affects health (even if they never develop Celiac), they'll be healthier people their whole lives.

happygirl Collaborator

I had both, positive blood work and a biopsy that showed spru in my stomach.

Aimee: Celiac is diagnosed through bloodwork/biopsy...however, Celiac damage is shown in your small intestine (where the villi are flattened due to Celiac- 'villous atrophy'), not your stomach. You could have irritation or other issues in your stomach, but damage to due Celiac is definitively found in your small intestine.

It sounds like you have gone through a lot....I am impressed that your doctor mentioned Celiac so "soon"-often, it takes a long time/never! I am happy that you found an answer, and now have found this board. I wish that there was something that I could do to make this easier. It sounds like you are going through a lot. It is hard to deal with this, plus the normal stresses of day to day life.

Given this new information (about eating gluten last week), basically all of my post before is not quite as relevant. If you have only been on the gluten free diet, and have eaten a massive amount of gluten in the past week: there is no reason to see any results, basically. Once you have screwed up: take a deep breath, and remember that we all make mistakes. HONESTLY. We really and truly all do. But, eating more gluten makes it exponentially worse. Any gluten is bad, but eating it in that amount is really bad :)! Even if you are not seeing "overt" symptoms, since you are a biopsy confirmed Celiac, it means that you will have intestinal damage when you eat gluten, even if you do not feel anything. (There are many cases of completely asymptomatic Celiacs, who have raging damage to their intestines). So, it will take you longer to recover, having eaten a massive amount of gluten plus the other stuff, than having just made the one mistake. Given the fact that you were "only" on the gluten-free free diet for about 2 months at that point....your body really has not had time to heal and adjust to this, to start re-absorbing nutrients correctly, etc. Studies have shown that tiny, tiny amounts of gluten can do damage (like, crumbs worth!), which is why maintaining a strict gluten free (not gluten lite!) diet is important. Tiny amounts of gluten can turn "on" our autoimmune system, and our goal is to stop turning it on, by staying gluten free.

Just so you know, there are specialty gluten free beers, including one that was just introduced in December----a more mainstream one, by Anheuiser-Busch called "Red Bridge." It might be worth it for you to find and try, so you have a good substitute. I haven't tried it yet, but there is a thread about it on here. Also, for Chinese food---I know making it at home is not exactly the "same" (trust me, I know!) as eating out, but there are gluten free soy sauces to use at home. La Choy makes one, as well as San-J (they have a regular and low-sodium one. Be careful to get the wheat-free one; they also make gluten-filled ones!)

By the way---check out the book listed in my signature. Open Original Shared Link is the website of the author's Celiac Clinic at Columbia University). It is a comprehensive guide that is research based, and recent (2006). It covers what Celiac does to our bodies, as well as related disorders (like diabetes).

I hope that you continue to find this board a place of support and information! We are here to help get you through the learning curve of the gluten free lifestyle :) as easily as possible. The good thing is that each day is a new day!

Laura

Nancym Enthusiast

Stick with it! Sorry you're not feeling vastly better already. I had some improvement in just a couple of days (with the bowels). But my arthritis, fatigue, muddle-headedness took months to get better.

I agree with the others, take the whole family gluten free and concentrate on eating foods that are not processed, like fruits, veggies, meats. Later on, when you're feeling much better you can introduce other things, slowly, taking careful note of how you feel.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Aimee D. Newbie

Thank you all so much. This has been even more helpful than I had anticipated!! I truely thought that the amount of gluten consumed made no difference on the recovery time or intensity of the ill effects. So in all actuality I can't even begin to blame cross contamination possibilities until I'm completely recovered from the chinese food and beer incident.

I do feel a little better today, no headache anyway. I am however extreamly constipated... no void in 4 days. Also I have been fog/mush headed my entire life, the tought of clear thinking is beyond my wildest dreams. Its difficult for me to get to the store with what I need (blood tester, pump, money, list, baby, sub zero cold weather gear...) much less find edible gluten free food in a timely mannor! Getting back inside the house with everything is a major accomplishment.

It's nice to have a little reassurance from you all though, I've been very overwhelmed lately...

Thanks,

Aimee

P.S. -26 degrees where I live today!

almostnrn Explorer

I really hope you are feeling better soon! Stick with it and check here often. There are so many knowledgeable and helpful people here. Also don't forget to check out the sections for recipes and gluten free "normal" foods that you can buy at the commissary. If you check with the manager they may be able to provide you a list of items that they stock that are gluten-free and may even order some items in for you. I have found that the commissary here at WPAFB is more than accomidating! As far as making your house gluten free...I would highly recommend it. All of our main meals such as dinner are always prepared gluten-free and I have to say that my kids seem to be much healthier and happier when they aren't eating a diet with gluten in it. Good luck and wishes for a speedy recovery!

Archived

This topic is now archived and is closed to further replies.

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to Paulaannefthimiou's topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Bob red mill gluten free oats

    2. - knitty kitty replied to SamAlvi's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      High TTG-IgG and Normal TTG-IgA

    3. - trents replied to SamAlvi's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      High TTG-IgG and Normal TTG-IgA

    4. - SamAlvi replied to SamAlvi's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      High TTG-IgG and Normal TTG-IgA

    5. - Jsingh replied to lizzie42's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      Son's legs shaking

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      132,868
    • Most Online (within 30 mins)
      7,748

    LMGarrison
    Newest Member
    LMGarrison
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • Scott Adams
      Oats naturally contain a protein called avenin, which is similar to the gluten proteins found in wheat, barley, and rye. While avenin is generally considered safe for most people with celiac disease, some individuals, around 5-10% of celiacs, may also have sensitivity to avenin, leading to symptoms similar to gluten exposure. You may fall into this category, and eliminating them is the best way to figure this out. Some people substitute gluten-free quinoa flakes for oats if they want a hot cereal substitute. If you are interested in summaries of scientific publications on the topic of oats and celiac disease, we have an entire category dedicated to it which is here: https://www.celiac.com/celiac-disease/oats-and-celiac-disease-are-they-gluten-free/   
    • knitty kitty
      @SamAlvi, It's common with anemia to have a lower tTg IgA antibodies than DGP IgG ones, but your high DGP IgG scores still point to Celiac disease.   Since a gluten challenge would pose further health damage, you may want to ask for a DNA test to see if you have any of the commonly known genes for Celiac disease.  Though having the genes for Celiac is not diagnostic in and of itself, taken with the antibody tests, the anemia and your reaction to gluten, it may be a confirmation you have Celiac disease.   Do discuss Gastrointestinal Beriberi with your doctors.  In Celiac disease, Gastrointestinal Beriberi is frequently overlooked by doctors.  The digestive system can be affected by localized Thiamine deficiency which causes symptoms consistent with yours.  Correction of nutritional deficiencies quickly is beneficial.  Benfotiamine, a form of thiamine, helps improve intestinal health.  All eight B vitamins, including Thiamine (Benfotiamine), should be supplemented because they all work together.   The B vitamins are needed in addition to iron to correct anemia.   Hope this helps!  Keep us posted on your progress!
    • trents
      Currently, there are no tests for NCGS. Celiac disease must first be ruled out and we do have testing for celiac disease. There are two primary test modalities for diagnosing celiac disease. One involves checking for antibodies in the blood. For the person with celiac disease, when gluten is ingested, it produces an autoimmune response in the lining of the small bowel which generates specific kinds of antibodies. Some people are IGA deficient and such that the IGA antibody tests done for celiac disease will have skewed results and cannot be trusted. In that case, there are IGG tests that can be ordered though, they aren't quite as specific for celiac disease as the IGA tests. But the possibility of IGA deficiency is why a "total IGA" test should always be ordered along with the TTG-IGA. The other modality is an endoscopy (scoping of the upper GI track) with a biopsy of the small bowel lining. The aforementioned autoimmune response produces inflammation in the small bowel lining which, over time, damages the structure of the lining. The biopsy is sent to a lab and microscopically analyzed for signs of this damage. If the damage is severe enough, it can often be spotted during the scoping itself. The endoscopy/biopsy is used as confirmation when the antibody results are positive, since there is a small chance that elevated antibody test scores can be caused by things other than celiac disease, particularly when the antibody test numbers are not particularly high. If the antibody test numbers are 10x normal or higher, physicians will sometimes declare an official diagnosis of celiac disease without an endoscopy/biopsy, particularly in the U.K. Some practitioners use stool tests to detect celiac disease but this modality is not widely recognized in the medical community as valid. Both celiac testing modalities outlined above require that you have been consuming generous amounts of gluten for weeks/months ahead of time. Many people make the mistake of experimenting with the gluten free diet or even reducing their gluten intake prior to testing. By doing so, they invalidate the testing because antibodies stop being produced, disappear from the blood and the lining of the small bowel begins to heal. So, then they are stuck in no man's land, wondering if they have celiac disease or NCGS. To resume gluten consumption, i.e., to undertake a "gluten challenge" is out of the question because their reaction to gluten is so strong that it would endanger their health. The lining of the small bowel is the place where all of the nutrition in the food we consume is absorbed. This lining is made up of billions of microscopically tiny fingerlike projections that create a tremendous nutrient absorption surface area. The inflammation caused by celiac disease wears down these fingers and greatly reduces the surface area needed for nutrient absorption. Thus, people with celiac disease often develop iron deficiency anemia and a host of other vitamin and mineral deficiencies. It is likely that many more people who have issues with gluten suffer from NCGS than from celiac disease. We actually know much more about the mechanism of celiac disease than we do about NCGS but some experts believe NCGS can transition into celiac disease.
    • SamAlvi
      Thank you for the clarification and for taking the time to explain the terminology so clearly. I really appreciate your insight, especially the distinction between celiac disease and NCGS and how anemia can point more toward celiac. This was very helpful for me.
    • Jsingh
      Hi,  My 7 year daughter has complained of this in the past, which I thought were part of her glutening symptom, but more recently I have come to figure out it's part of her histamine overload symptom. This one symptom was part of her broader profile, which included irritability, extreme hunger, confusion, post-nasal drip. You might want to look up "histamine intolerance". I wish I had known of this at the time of her diagnosis, life would have been much easier.  I hope you are able to figure out. 
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.